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HARVARD Citation
Jones, K. et al. (n.d.). A homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromes. American journal of medical genetics. pp. 2691-2696. [Online].
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Jones, K. et al. (n.d.). A homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromes. American journal of medical genetics. pp. 2691-2696. [Online].